Guest guest Posted March 10, 2008 Report Share Posted March 10, 2008 Dear Ron, I'm re-reading your message and wanted to add a few things to what I wrote before. I wold never say what you should do, so take the following very random thoughts as just that, okay? In addition to helping mobility, tremors, etc., Sinemet acts as a stimulant. As such, it can greatly increase confusion, delusions, anxiety, agitation, etc. That' s what it did to my mom, after being on 25/100 4X/day for 4+ years. Her brain just couldn't take that much stimulation. She has done better on Provigil, which doesn't affect the CNS in the same way, but aid salertness and muscle movement. Although it like all these meds is strong, it's a " safer " drug for my mom. Of course, Sinemet - and Pro, too, for that matter - have other effects I didn't mention. I'd think a lot of evaluating your mom depends on the dosages of her other meds, when you give them, and details of what you're seeing. Are there any contraindications? Does she seem " zoned out? " What's her alertness level? Do any behaviors seem tied (within a few hours) to when you give the various meds? What does her talking being not the greatest actually mean in action? Frequency and fluency? What about her level of cognition? Does she know you? Have any memory retrieval? What are you goals for her at this point? Are you in a position to do some reasonable meds shifts to see what might happen? All those questions the MD asks we can ask ourselves and each other as we investigate our options. Of course you want as much quality of life as possible, and while the disease keeps carrying our loved ones away, we can be vigilant about meds and other treatments - adjusting them when it seems we will get improvement without doing harm. After LBD, I know much better what " a delicate balance " means! Let's stay in touch. Lin Ron wrote: Dear Courage and Lin, I hope all is well.I was reading your posts and saw that you had both cut your moms sinemet back at some point.Mom was origionally diagnosed with parkinsons and she is all the way up to 25/250 pills 4 times a day.I also know the drawbacks from it but it seems like thats the one pill that when its a minute late she really gets antsy for it.She doesnt walk at all on her own with out help and her life lately is sitting in her chair, getting help to the bathroom and kitchen and help to bed.She still smiles and laughs at times but I wonder how much quality of life she really has anymore.I was wondering about the damage the sinemet may be doing, and if I were to cut it back from such a strong dose what I should expect, her talking isnt the greatest and she cant write or put a ring on her finger or small things like that.Im just wondering out loud I guess if there is more quality of life to be given or if this is where we are and its only down hill.II swear by the aricept and seroquel and even the paxil as she hardly ever cries anymore ore gets delusional, but I wonder about the sinemet.Just wondered about everyones take on it.I hope all is well Ron ________________________________________________________________________________\ ____ Never miss a thing. Make Yahoo your home page. http://www.yahoo.com/r/hs Welcome to LBDcaregivers. Quote Link to comment Share on other sites More sharing options...
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